annotate/svm_annotation

Description

Automated cell type annotation tool for scRNA-seq datasets on the basis of SVMs.

Type

python_script

License

MIT

Contributors

Run this component

Run the following command to execute this component with Nextflow:

cat > params.yaml <<'EOM'  
modality: [ "rna" ]  
input_reference_gene_overlap: [ 100 ]  
output: "$id.$key.output.h5mu"  
output_obs_prediction: [ "svm_pred" ]  
output_obs_probability: [ "svm_probability" ]  
feature_selection: [ true ]  
max_iter: [ 5000 ]  
c_reg: [ 1 ]  
class_weight: [ "balanced" ]  
id: "run"  
publish_dir: "output/"  
EOM

nextflow run https://packages.viash-hub.com/vsh/openpipeline.git \  
  -revision v3.0.0 \  
  -main-script target/nextflow/annotate/svm_annotation/main.nf \  
  -params-file params.yaml  

Inputs

Name
Type & Properties
--input
file
required
--modality
string
--input_layer
string
--input_var_gene_names
string
--input_reference_gene_overlap
integer

Reference

Name
Type & Properties
--reference
file
--reference_layer
string
--reference_obs_target
string
required
--reference_var_gene_names
string
--reference_var_input
string

Outputs

Name
Type & Properties
--output
file
output
--output_obs_prediction
string
--output_obs_probability
string
--output_compression
string

Model arguments

Name
Type & Properties
--model
file
--feature_selection
boolean
--max_iter
integer
--c_reg
double
--class_weight
string

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